US2100798A - Condensation products of carbenium compounds and process of preparing the same - Google Patents

Description

Patented Nov. 30, 1937 UNITED STATES PATENT OFFICE CONDENSATION PRODUCTS OF CARBE- NIUM COMPOUNDS AND PROCESS OF PRE- PARING THE SAME Walther Dilthey and Ferdinand Quint, Bonn-onthe-Ithine, Germany, assignors to I. G. Farbenindustrie Aktiengesellschaft, Frankfort-onthe -Main, Germany No Drawing. Application April 27, 1934, Serial No. 722,814. In Germany May 2, 1933 15 Claims.

wherein Y represents hydrogen, the hydroxyl group or the radical of an acid. X represents oxygen, sulfur or an NI-I- or Naryl group and wherein there is contained a further benzene nucleus condensed in the 7.8-positions of the formula or in ortho-positions of the nucleus R which may contain substituents and a further benzene nucleus may be condensed in the Lil-positions of the formula, with a hydrogen acceptor, such as oxygen, for instance, in the form of air, or aluminium chloride or zinc chloride in the manner described in the following examples.

By the action of oxygen, aluminium chloride or zinc chloride the substances of Formula I lose hydrogen and undergo an inner ring closure, for instance, probably according to the following formulae:

dehydrogenating r agent double inner ring closure and formation of a product of the following formula:

but nothing definite can be said about the constitution of the dehydrogenation product. The dehydrogenation in some cases occurs by itself whereby there is obtained as reaction product the corresponding methane probably according to the following formulae:

V VI

The dehydrogenation always occurs if a suitable hydrogen acceptor is present and is favorably influenced by supply of energy in form of heat or light (sun-light or an artificial source of light). As hydrogen acceptor the most important is oxygen, for instance, in the form of air, but other oxidizing or dehydrogenating agents may also be used, among them, quinone, methylene-blue or ferric salts. It is also possible to effect the dehydrogenation by means of zinc chloride or aluminium chloride. In the case of zinc chloride the better yields are obtained when the carbenium compound is a salt, for instance, a perchlorate, and in the case of aluminium chloride the better yields are obtained when the carbenium compound is a carbinol.

Since the methanes of the compounds of Formula I (wherein Y stands for hydrogen) are easily transformed into the carbinols or their salts by the action of oxidizing agents, there may also be used in the present process the methanes of the carbenium compounds as starting materials.

The salts obtainable according to the new process may be transformed into the corresponding carbinols by means of alkalies. The new prodnets are dyestufis or intermediate products for the manufacture of dyestuffs. For instance, suitable auxochromic groups may be introduced with formation of dyestuffs, either before or after the dehydrogenation. Nothing definite can be said about the constitution of the final products.

It is also possible, for instance, that during the action of oxygen the latter is absorbed, perhaps with simultaneous dehydrogenation.

The following examples serve to illustrate the invention. The parts are by weight unless stated otherwise.

(1) 8.7 grams of 9-(4-methylphenyl) -dibenz0- xanthenium-chloride of the following formula:

are intimately triturated with 15 grams of aluminium chloride and heated together in a suitable jar on the oilbath. At somewhat above C., the whole melts to a deep-blue mass. The said temperature is maintained until the mass which at first foams violently, is at rest. The temperature is then raised to 200 C., while stirring fre quently, and maintained for further two hours. The solidified mass is introduced into 1% liters of hot water and dissolved, filtered so as to eliminate a small residue and 500 cc. of fuming hydrochloric acid are added to the hot liquid.

The dehydrO-S-( l-methylphenyl) 1,2,7,8-dibenzo-xantheniumchloride of the following probable formula: 7

thus obtained, settles after cooling in the form of a fine sludge which is collected on a suction filter made from sintered material and is washed with a mixture of alcoho1 and ether. A violet powder is obtained. The yield amounts to 6 ams.

(2) 15 grams of 9-phenyl-l,2,7,8-dibenzo-xantheniumperchlorate (cf. Gomberg and Cone, Annalen der Chemie, vol. 3'70, page 168) are triturated in a mortar with grams of zinc chloride and heated together to about 500 C. for 1 to 2 hours whereby the mass which foams at first violently, is at rest. The bluish-black melt is purified by boiling it several times with glacial acetic acid. 15 grams of a bluish-black powder probably of the following constitution:

are obtained.

(3) 1 mol, of 9-phenyl-dibenzo-xanthene of the formula:

(cf. Claisen, Annalen der Chemie, vol. 237, page 266) is dissolved in such a quantity of glacial acetic acid, mixed with hydrochloric acid, as is,

no longer increases. The yield is nearly quantitative. Artificial light may also be used instead of sunlight.

(4) 5 grams of 9-phenyl-7,8-benzo-xantheniumperchlorate of the formula:

are exposed in a glacial acetic acid solution or suspension to the sunlight or to artificial light and then boiled, oxygen or air being passed through. 'After some hours the transformation is finished, the yellow salt is completely converted into the brown red crystalline dehydro-Q-phenylbenzo-xantheniumperchlorate, melting at 286 C.

6 grams of phenyldinaphthoacridine (of. F. Ullman-n and A. Fetvajian, Berichte der deutschen chemischen Gesellschaft, vol. 36, page 1030, 1903-) are mixed with 14 grams of aluminium chloride and heated in the oil bath for 2% hours to 200 C. After cooling, the melt is extracted by boiling with 750 cc, of water and the new product is precipitated from the solution by means of hydrogen chloride. The yield of dark-red dehydrophenyldinaphthoacridine-chloride of the following probable formula:

amounts to 5-6 grams.

(6) 6 grams of phenyldinaphtho-acridiniumperchlorate in 450 cc. of nitrobenzene are exposed to direct sunlight until the precipitation of darkred crystals of perchlorate of the dehydro com pound is finished. The yield depends on the duration of the exposure, amounts however easily to 3-4 grams.

('7) A glacial acetic acid solution of N-phenylms-phenyl- 1,2,7 ,S-dibenzo acricliniumchloride of the following constitution:

assumes in daylight in the course of several daysrapidly in the sun-a brown-red color whereby the original bright green-yellow fluorescence almost disappears. A test portion is taken from the solution, much diluted with glacial acetic acid and filtered. When the filtrate shows a pale-pink color, the dehydration is finished. The dehydro-N-phenyl-ms-phenyl- 1,2,'7,8-dibenzo-acridiniumchloride, probably of the following constitution:

I l I I I I A thus obtained, is precipitated with ether. It forms brown dark-brilliant leaflets which, when recrystallized from acetic anhydride, are obtained in the form of orange-red leaflets having a yellow surface-luster. They dissolve very readily in water to an orange-red solution having a fluorescence of the same color which turns greenish-yellow on addition of glacial acetic acid.

(8) 5 grams of ms-naphthyl-xanthenol of the formula:

being a black powder which dissolves in glacial acetic acid only to a very small extent to a dirty orange fluorescent solution. By addition of concentrated hydrochloric acid, the solution becomes intensely blue-green whereby the fluorescence turns red.

(9) To a solution of 1 gram of B,B-dinaphthylsulfide in 2 grams of benzoyl-chloride 3 grams of aluminium chloride are added in small portions. When the evolution of gas and the foaming, are

finished, the whole is heated for a further 1%,, hours .at 200 C., the bluish-black cooled melt is extracted several times by boiling with water (total quantity 150 cc.) until no more dyestuif dissolves; an equal quantity of glacial acetic acid is added to the solution and the whole is mixed hot with a glacial acetic acid solution of picric acid. On cooling, the dehydro-ms-phenyl- 1,2,'7,8-dibenzo-thioxanthenium-picrate of the following probable formula:

(cf. Dischendorfer and Nesitka, Monatshefte der Chemie, vol. 50, page 27) are introduced at a temperature not exceeding 130 C. into a mixture of parts of aluminium chloride and 30 parts of sodium chloride. After stirring for 5 hours at C. to 150 0., the whole is poured into 2000 parts of water, the Whole is heated to boiling, filtered by suction, the residue is extracted by boiling again with 2000 parts of water and the dyestufi obtained is precipitated from the combined red filtrates by means of hydrochloric acid. In order to purify the dyestufi, it may be dissolved in water and again precipitated with hydrochloric acid. The dyestufi thus obtainable, which probably corresponds to the following constitution:

Nfllz dissolves in water to'a wine-red solution and dyes cotton, tanned cotton, loaded and unloaded silk intense red tints of good fastness to light.

(11) 40 parts of m-nitrophenyl-dinaphthopyran of the formula:

(cf. Dischendorfer, Monatsheite der Chemie, vol. 49, page are introduced at 110 C. to 130 G. into a mixture of 120 parts of aluminium chloride and 30 parts of sodium chloride and, while stirring vigorously, the temperature is maintained for 6 hours at 130 C. The whole is then poured into 3000 parts of water, heated to boiling for about 10 minutes, filtered by suction, the residue is extracted again by boiling with 2000 parts of water and the dyestuff is precipitated from the combined light-green filtrates by means of hydrochloric acid. After extraction by boiling with concentrated hydrochloric acid (37% strength), the hydrochloride of the amine of the following probable formula: 7 I

is obtained in the form of a micro-crystalline powder. The dyestufi which is readily soluble in warm water easily dyes cotton and tanned cotton clear green tints which are fast to light and dyes loaded and unloaded silk very clear yellow-green tints of very good fastness to water, washing and to perspiration as well as of a good fastness to light.

We claim:

1. The process which comprises heating at about 500 C. for about two hours a mixture of 9-phenyl-1,2,7,8-dibenzo-xanthenium perchlorate with zinc chloride.

2. The process which comprises heating, While stirring, at about 130 C. to about C. for about 5 hours a mixture of para-nitrophenyl-dinaphtho-pyranol with aluminium chloride and sodium chloride.

3. The process which comprises introducing para-nitro-phenyl-dinaphtho-pyranol into a mixture of aluminium chloride and sodium chloride at a temperature not exceeding about 130 C., heating the whole, while stirring, at about 130 C. to about 150 C. for about 5 hours, and decomposing the reaction mass with water.

4. The process which comprises heating, while stirring, at about 130 C. for about 6 hours a mixture of meta-nitrophenyl-dinaphtho-pyran with aluminium chloride and sodium chloride.

5. The process which comprises introducing meta-nitrophenyl-dinaphtho-pyran into a mix- 'ture of aluminium chloride and sodium chloride at a temperature not exceeding about 130 C.,"

heating the whole, while stirring, at about 130 C. for about 6 hours, and decomposing the reaction mass with water.

wherein Y represents a member of the group consisting of hydrogen, hydroxyl and the radical of an acid and X represents a member of the group consisting of oxygen, sulfur, imino and arylimino.

10. The process which comprises heating in the presence of aluminium chloride, a member of the group consisting of compounds of the general formulae:

6. The compound of the following formula:

being a bluish-black powder, Y

'7. The compound of the following formula:

- NH: I I

and

wherein Y represents a member of the group consisting of hydrogen, hydroxyl and the radical of an acid and X represents a member of the group consisting of oxygen, sulfur, imino, and arylimino.

\O 11. The process which comprises heating in the presence of aluminium chloride, a member of the group consisting of compounds of the general formulae:

being readily soluble in warm water, dyeing easily cotton and tanned cotton clear green tints which are fast to light and dyeing loaded and unloaded silk very clear yellow-green tints of very good fastness to water, washing and to perspiration as well as of good fastness to light.

9. The process which comprises heating in the presence of an agent of the group consisting of aluminium chloride, zinc chloride, oxygen, qui- A q none, methylene blue and ferric salts, a member I of the group consisting of compounds of the general formulae:

Y Y o o and 1 x X 7 and wherein Y represents a member of the group consisting of hydrogen, hydroxyl and the radical X/ of an acid.

12. The process which comprises heating in the presence of aluminium chloride, a compound of the general formula:

wherein Y represents a member of the group consisting of hydrogen, hydroxyl, and the radical of an acid.

14. The compounds of the general formula:

wherein Y represents a member of the group consisting of hydrogen, hydroxyl, and the radical of an acid.

15. The compounds of the general formula:

wherein X represents a member of the group consisting of oxygen, sulfur, imino and arylimino and Y represents a member of the group consisting of hydrogen, hydroxyl and the radical of an acid.

- WALTHER DILTHEY.

FERDINAND QUINT.